Pharma MES & MBR Consultant

The Pharma MES & MBR Consultant will inspire customers through technology, using knowledge of EBRs, pharmaceutical industry processes, regulations, GxP compliance, cloud computing, and SaaS. Responsibilities include providing consulting on the implementation and use of Aizon’s EBR software (Execute), participating in projects and Proofs of Value, delivering training, conducting gap assessments of clients' Master Batch Recipes (MBR), designing conversion strategies, ensuring GxP compliance, supporting documentation and validation, identifying new business opportunities, supporting pre-sales, collaborating with solution architects and clients, and mapping system integrations. The role requires a strong understanding of pharmaceutical manufacturing processes, GxP, FDA, and global regulations, excellent communication skills, ability to work independently and in teams, and willingness to travel. Preferred qualifications include experience in EBR implementation/validation, system integration, programming, and additional languages.

The Pharma MES & MBR Consultant will provide consulting services to pharmaceutical clients on the implementation of Aizon’s EBR software, ensuring successful adoption and client satisfaction.

Spain

The Pharma MES & MBR Consultant will inspire customers through technology, using knowledge of EBRs, pharmaceutical industry processes, regulations, GxP compliance, cloud computing, and SaaS. Responsibilities include providing consulting on the implementation and use of Aizon’s EBR software (Execute), participating in projects and Proofs of Value, delivering training, conducting gap assessments of clients' Master Batch Recipes (MBR), designing conversion strategies, ensuring GxP compliance, supporting documentation and validation, identifying new business opportunities, supporting pre-sales, collaborating with solution architects and clients, and mapping system integrations. The role requires a strong understanding of pharmaceutical manufacturing processes, GxP, FDA, and global regulations, excellent communication skills, ability to work independently and in teams, and willingness to travel. Preferred qualifications include experience in EBR implementation/validation, system integration, programming, and additional languages.Requirements:<ul><li> Minimum MSc in Pharmaceuticals, Biotechnology, Chemistry, Engineering, or Computer Science.</li><li> At least 3+ years in a customer-facing role participating in client projects.</li><li> 3+ years of experience in pharmaceutical, biotech, or regulated industries, focusing on manufacturing processes.</li><li> Strong understanding of GxP, FDA, and global regulatory requirements for EBRs.</li><li> Excellent communication and interpersonal skills.</li><li> Ability to work independently and as part of a team.</li><li> Ability to meet deadlines and deliver high-quality work.</li><li> Ability to understand business requirements and translate into software configuration.</li><li> Availability to travel for client visits.</li><li> Proficiency in spoken and written English.</li></ul>Benefits:<ul><li> Competitive salary (according to experience/skills).</li><li> Equity, bonuses, and stock options.</li><li> Flexible schedule with intensive Fridays.</li><li> Language training courses.</li><li> Medical & Dental Insurance.</li><li> Internal training and certifications.</li><li> Flexible remuneration options.</li><li> Career plan and salary reviews.</li><li> Monthly team-building activities.</li><li> Top-notch tech equipment (Mac).</li><li> International, collaborative work environment.</li><li> Opportunities for personal and professional growth.</li><li> Inclusive workplace respecting diversity.</li><li> Support for applicants requiring assistance due to disability.</li></ul>

Aizon

Pharma MES & MBR Consultant The Pharma MES & MBR Consultant will provide consulting services to pharmaceutical clients on the implementation of Aizon’s EBR software, ensuring successful adoption and client satisfaction. The Pharma MES & MBR Consultant will inspire customers through technology, using knowledge of EBRs, pharmaceutical industry processes, regulations, GxP compliance, cloud computing, and SaaS. Responsibilities include providing consulting on the implementation and use of Aizon’s EBR software (Execute), participating in projects and Proofs of Value, delivering training, conducting gap assessments of clients' Master Batch Recipes (MBR), designing conversion strategies, ensuring GxP compliance, supporting documentation and validation, identifying new business opportunities, supporting pre-sales, collaborating with solution architects and clients, and mapping system integrations. The role requires a strong understanding of pharmaceutical manufacturing processes, GxP, FDA, and global regulations, excellent communication skills, ability to work independently and in teams, and willingness to travel. Preferred qualifications include experience in EBR implementation/validation, system integration, programming, and additional languages. Pharma MES & MBR Consultant Consultant Aizon pharmaceutical-manufacturing technology-information-and-internet software-development it-services-and-it-consulting data-infrastructure-and-analytics Barcelona

This role involves guiding clients through the implementation of Aizon’s EBR software, conducting gap assessments, delivering training, and supporting compliance in regulated environments. The consultant will collaborate with various teams to optimize software deployment and contribute to business growth.

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